JPH0717860B2 - イソインドリン顔料の調色法 - Google Patents

イソインドリン顔料の調色法

Info

Publication number: JPH0717860B2
Authority: JP; Japan
Prior art keywords: pigment; acid; isoindoline pigment; isoindoline; water
Prior art date: 1985-07-05
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Lifetime

Application number

JP61152841A

Other languages

English (en)

Japanese (ja)

Other versions

JPS6210169A (ja

Inventor

ウオルフガング・ロツチユ

ラインハルト・ケムパー

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

BASF SE

Original Assignee

BASF SE

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1985-07-05

Filing date

1986-07-01

Publication date

1995-03-01

1986-07-01 Application filed by BASF SE filed Critical BASF SE

1987-01-19 Publication of JPS6210169A publication Critical patent/JPS6210169A/ja

1995-03-01 Publication of JPH0717860B2 publication Critical patent/JPH0717860B2/ja

2010-03-01 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

239000000049 pigment Substances 0.000 title claims description 68
238000000034 method Methods 0.000 title claims description 30
GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 title claims description 21
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 25
239000000203 mixture Substances 0.000 claims description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 12
239000005711 Benzoic acid Substances 0.000 claims description 11
235000010233 benzoic acid Nutrition 0.000 claims description 11
-1 N-phenylcarbamoyl group Chemical group 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 6
239000000725 suspension Substances 0.000 claims description 4
125000004174 2-benzimidazolyl group Chemical group [H]N1C(*)=NC2=C([H])C([H])=C([H])C([H])=C12 0.000 claims description 2
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 2
150000001991 dicarboxylic acids Chemical class 0.000 claims 4
150000002763 monocarboxylic acids Chemical class 0.000 claims 4
239000011541 reaction mixture Substances 0.000 claims 2
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims 1
239000002245 particle Substances 0.000 description 7
239000000047 product Substances 0.000 description 5
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 4
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 4
238000004040 coloring Methods 0.000 description 4
238000010438 heat treatment Methods 0.000 description 4
239000002966 varnish Substances 0.000 description 4
AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
RZVCEPSDYHAHLX-UHFFFAOYSA-N 3-iminoisoindol-1-amine Chemical compound C1=CC=C2C(N)=NC(=N)C2=C1 RZVCEPSDYHAHLX-UHFFFAOYSA-N 0.000 description 2
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
239000007900 aqueous suspension Substances 0.000 description 2
HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 description 2
239000003086 colorant Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
239000001053 orange pigment Substances 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
239000000243 solution Substances 0.000 description 2
HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000001058 brown pigment Substances 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000012535 impurity Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
239000011164 primary particle Substances 0.000 description 1
238000003908 quality control method Methods 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
101150035983 str1 gene Proteins 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
238000010189 synthetic method Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000001052 yellow pigment Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0001—Post-treatment of organic pigments or dyes
- C09B67/0017—Influencing the physical properties by treatment with an acid, H2SO4
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
- C09B57/04—Isoindoline dyes

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Paints Or Removers (AREA)
Pigments, Carbon Blacks, Or Wood Stains (AREA)

JP61152841A 1985-07-05 1986-07-01 イソインドリン顔料の調色法 Expired - Lifetime JPH0717860B2 (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE3524110.1		1985-07-05
DE3524110		1985-07-05

Publications (2)

Publication Number	Publication Date
JPS6210169A JPS6210169A (ja)	1987-01-19
JPH0717860B2 true JPH0717860B2 (ja)	1995-03-01

Family

ID=6275075

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP61152841A Expired - Lifetime JPH0717860B2 (ja)	1985-07-05	1986-07-01	イソインドリン顔料の調色法

Country Status (5)

Country	Link
US (1)	US4845214A (de)
JP (1)	JPH0717860B2 (de)
CH (1)	CH668980A5 (de)
DE (1)	DE3622322C2 (de)
GB (1)	GB2177105B (de)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3935858A1 (de) *	1989-10-27	1991-05-02	Bayer Ag	Verfahren zur herstellung von pigmenten auf isoindolbasis
US6143067A (en) *	1998-01-28	2000-11-07	Ciba Specialty Chemicals Corporation	Isoindoline pigment having improved low shear dispersibility
US7009098B2 (en) *	2004-03-26	2006-03-07	Woodstock Percussion, Inc.	Water activated chiming device
ATE481454T1 (de) *	2006-07-18	2010-10-15	Basf Se	Isoindolinpigmente
WO2009074533A2 (en) *	2007-12-10	2009-06-18	Basf Se	Isometric isoindoline yellow pigment
TWI754733B (zh) *	2017-03-29	2022-02-11	日商住友化學股份有限公司	異吲哚啉色素及其製造方法
JP7055677B2 (ja) *	2017-03-29	2022-04-18	住友化学株式会社	イソインドリン色素の製造方法
EP3798271A1 (de) *	2019-09-30	2021-03-31	BASF Colors & Effects GmbH	Isoindolinderivate
CN115916909B (zh) *	2020-07-15	2024-05-14	爱天思株式会社	颜料及着色组合物、涂料、油墨、油墨组、印刷物及包装材料
CN113943495B (zh) *	2021-11-02	2023-10-27	江苏丽王科技股份有限公司	一种异吲哚啉颜料及其制备方法

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3127412A (en) *	1959-09-29	1964-03-31	Ciba Ltd	Process for conditioning pigments
ES261340A1 (es) *	1959-09-29	1961-05-16	Ciba Geigy	Procedimiento para acondicionar pigmentos organicos
US3923806A (en) *	1971-05-03	1975-12-02	Basf Ag	Disperse dyes based on isoindolene derivatives
JPS5131726A (ja) *	1974-09-12	1976-03-18	Sumitomo Chemical Co	Fuyoseiazoganryonoseiho
JPS581151B2 (ja) *	1975-07-03	1983-01-10	大日精化工業株式会社	ガンリヨウノケツシヨウセイシツヘンカンホウホウ
DE2628409C3 (de) *	1976-06-24	1986-10-02	Basf Ag, 6700 Ludwigshafen	Verfahren zur Herstellung von Pigmentfarbstoffen
CH625542A5 (de) *	1977-04-07	1981-09-30	Ciba Geigy Ag
DE2800815C2 (de) *	1978-01-10	1986-12-11	Basf Ag, 6700 Ludwigshafen	Verfahren zur Herstellung leicht verteilbarer und deckender Isoindolinpigmentfarbstoffe
JPS5667370A (en) *	1979-11-06	1981-06-06	Sumitomo Chem Co Ltd	Preparation of azo pigment
DE3007300A1 (de) *	1980-02-27	1981-09-10	Basf Ag, 6700 Ludwigshafen	Neue isoindolinfarbstoffe
EP0038548A3 (de) *	1980-04-21	1982-10-06	Mobay Chemical Corporation	Verfahren zur Konditionierung von organischen Pigmenten
DE3208218A1 (de) *	1982-03-06	1983-09-08	Basf Ag, 6700 Ludwigshafen	Isoindolinfarbstoffe und deren verwendung
DE3327563A1 (de) *	1983-07-30	1985-02-07	Basf Ag, 6700 Ludwigshafen	Farbstarke isoindolinpigmente, deren herstellung und verwendung
DE3327564A1 (de) *	1983-07-30	1985-02-07	Basf Ag, 6700 Ludwigshafen	Lasierende, farbstarke isoindolinpigmente, deren herstellung und verwendung
DE3432319A1 (de) *	1984-09-03	1986-03-13	Hoechst Ag, 6230 Frankfurt	Verfahren zur herstellung organischer pigmente mit hervorragenden anwendungstechnischen eigenschaften
DE3442118A1 (de) *	1984-11-17	1986-05-22	Basf Ag, 6700 Ludwigshafen	Verfahren zur herstellung von farbstarken polyhalogenkupferphthalocyaninen
CH669388A5 (de) *	1985-07-09	1989-03-15	Basf Ag

1986
- 1986-06-13 CH CH2414/86A patent/CH668980A5/de not_active IP Right Cessation
- 1986-07-01 JP JP61152841A patent/JPH0717860B2/ja not_active Expired - Lifetime
- 1986-07-03 DE DE3622322A patent/DE3622322C2/de not_active Expired - Fee Related
- 1986-07-04 GB GB8616391A patent/GB2177105B/en not_active Expired
- 1986-07-07 US US06/882,359 patent/US4845214A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
DE3622322C2 (de)	1996-09-19
GB8616391D0 (en)	1986-08-13
CH668980A5 (de)	1989-02-15
DE3622322A1 (de)	1987-01-08
GB2177105B (en)	1989-07-19
GB2177105A (en)	1987-01-14
JPS6210169A (ja)	1987-01-19
US4845214A (en)	1989-07-04

Publication	Publication Date	Title
US3615800A (en)	1971-10-26	Process for converting perylene-3 4 9 10-tetracarboxylic acid diimide into a pigment form having valuable coloristic properties
JPH0717860B2 (ja)	1995-03-01	イソインドリン顔料の調色法
US3836379A (en)	1974-09-17	Quinacridone pigment mixtures and process for preparing them
EP0017214A1 (de)	1980-10-15	Neue Isoindolinfarbstoffe und deren Verwendung
JPH0674385B2 (ja)	1994-09-21	置換もしくは非置換のキナクリドンの調製方法
US3341345A (en)	1967-09-12	Solid solutions of a quinacridone and n, n'-diaryl-diamino compounds
JPS6328109B2 (de)	1988-06-07
US3697526A (en)	1972-10-10	Crystalline perylenetetracarboxylic acid dibenzoylhydrazide
US4097510A (en)	1978-06-27	Water-insoluble nickel-complex disazo methine compounds
US4099980A (en)	1978-07-11	Process for producing gamma quinacridone solid solutions
DE2130790C3 (de)	1978-04-06	Basische Farbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung
US2965644A (en)	1960-12-20	Dyestuffs of the naphthoylene-arylimidazol-peri-dicarboxylic acid series
US2837528A (en)	1958-06-03	Phthalocyanine pigments
US3741970A (en)	1973-06-26	Linear alkyl-amido transquinacridone pigments
JPH09110867A (ja)	1997-04-28	キナクリドン系化合物の製造法及び精製法
US3749726A (en)	1973-07-31	Linear alkyl-amido trans-quinacridone pigments
DE2025291B2 (de)	1973-08-02	Benzoxanthen- und benzothioxanthenfarbstoffe und verfahren zu ihrer herstellung
JPS6241267B2 (de)	1987-09-02
JP2820238B2 (ja)	1998-11-05	複素環式ピグメントおよび染料
US3793327A (en)	1974-02-19	Alpha-2,9-difluoroquinacridone
US4088651A (en)	1978-05-09	Acylamino quinophthalone compounds
JPH0569141B2 (de)	1993-09-30
EP0003565A1 (de)	1979-08-22	Von Isatinderivaten abgeleitete Dispersionsfarbstoffe, Verfahren zu deren Herstellung und deren Verwendung zum Färben und Bedrucken synthetischer Fasern
EP0015570B1 (de)	1982-12-22	Isoindolinpigmente und deren Verwendung
US4723023A (en)	1988-02-02	Isoindoline dyes